| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58007037-58007390 | Common:1; Rare:138 | ||||
| chr17:58007604-58007778 | Rare:43 | ||||
| chr17:58219201-58219372 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):5 | ||||
| chr17:58352125-58352320 | Common:4; Rare:85 | ||||
| chr17:58692357-58692733 | Common:2; Rare:160; Clinvar:26; Clinvar (benign):24 | ||||
| chr17:59106623-59106999 | Common:3; Rare:116; Clinvar:6; Clinvar (benign):4 | ||||
| chr17:59154972-59155025 | Rare:24 | ||||
| chr17:59155115-59155362 | Common:1; Rare:68 | ||||
| chr17:59155395-59155793 | Rare:99 | ||||
| chr17:59220387-59220636 | Common:4; Rare:70 | ||||
| chr17:59565469-59565781 | Common:2; Rare:114 | ||||
| chr17:59619181-59619322 | Rare:35 | ||||
| chr17:59619534-59619734 | Common:2; Rare:60 | ||||
| chr17:59619782-59620139 | Common:1; Rare:129 | ||||
| chr17:59655730-59656028 | Rare:48 |